Microwave-mediated nickel-catalyzed cyclotrimerization reactions: total synthesis of illudinine

J Org Chem. 2008 Jan 4;73(1):342-5. doi: 10.1021/jo7020955. Epub 2007 Dec 5.

Abstract

Rapid and efficient [2 + 2 + 2] cyclotrimerization reactions were discovered through the application of microwave irradiation in conjunction with a Ni(CO)(2)(PPh(3))(2) catalyst. This enables the facile construction of highly substituted indane, isoindoline, and tetraline core structures. The developed microwave-mediated Ni-catalyzed cyclotrimerization reaction was employed as the key step in a concise synthesis of the isoquinoline natural product illudinine. This represents the first example of a Ni-catalyzed cyclotrimerization reaction in total synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Cyclization
  • Microwaves*
  • Molecular Structure
  • Nickel / chemistry*
  • Nickel / radiation effects*
  • Organometallic Compounds / chemistry*
  • Organometallic Compounds / radiation effects*
  • Sesquiterpenes / chemical synthesis*
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / radiation effects*
  • Stereoisomerism

Substances

  • Organometallic Compounds
  • Sesquiterpenes
  • Nickel
  • illudinine